methyl 3,4-di-O-benzyl-6-O-triphenylmethyl-2-acetamido-2-deoxy-a-D-glucopyranoside

Base Information

Chemical Name:methyl 3,4-di-O-benzyl-6-O-triphenylmethyl-2-acetamido-2-deoxy-a-D-glucopyranoside
CAS No.:69892-50-8
Molecular Formula:C₄₂H₄₃NO₆
Molecular Weight:657.807
Hs Code.:

Synonyms:methyl 3,4-di-O-benzyl-6-O-triphenylmethyl-2-acetamido-2-deoxy-a-D-glucopyranoside

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of methyl 3,4-di-O-benzyl-6-O-triphenylmethyl-2-acetamido-2-deoxy-a-D-glucopyranoside

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Technology Process of methyl 3,4-di-O-benzyl-6-O-triphenylmethyl-2-acetamido-2-deoxy-a-D-glucopyranoside

There total 13 articles about methyl 3,4-di-O-benzyl-6-O-triphenylmethyl-2-acetamido-2-deoxy-a-D-glucopyranoside which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 92.0%

: 100-44-7
benzyl chloride

: 50908-05-9
methyl 6-O-triphenylmethyl-2-acetamido-2-deoxy-α-D-glucopyranoside

: 69892-50-8
methyl 3,4-di-O-benzyl-6-O-triphenylmethyl-2-acetamido-2-deoxy-a-D-glucopyranoside

Guidance literature:: With potassium hydroxide; In 1,4-dioxane; at 80 ℃; for 3h;

Reference yield: 87.0%

: 100-39-0
benzyl bromide

: 50908-05-9
methyl 6-O-triphenylmethyl-2-acetamido-2-deoxy-α-D-glucopyranoside

: 69892-50-8
methyl 3,4-di-O-benzyl-6-O-triphenylmethyl-2-acetamido-2-deoxy-a-D-glucopyranoside

Guidance literature:: With sodium hydride;
DOI:10.1016/j.bmc.2021.116501

Reference yield:

: 76-83-5
trityl chloride

: 69892-50-8
methyl 3,4-di-O-benzyl-6-O-triphenylmethyl-2-acetamido-2-deoxy-a-D-glucopyranoside

Guidance literature:: Multi-step reaction with 2 steps

1: 62 percent / pyridine / 120 h

2: 92 percent / KOH / dioxane / 3 h / 80 °C

With pyridine; potassium hydroxide; In 1,4-dioxane;